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Items: 1 to 20 of 82

1.

TFE3 Xp11.2 Translocation Renal Cell Carcinoma Mouse Model Reveals Novel Therapeutic Targets and Identifies GPNMB as a Diagnostic Marker for Human Disease.

Baba M, Furuya M, Motoshima T, Lang M, Funasaki S, Ma W, Sun HW, Hasumi H, Huang Y, Kato I, Kadomatsu T, Satou Y, Morris N, Karim BO, Ileva L, Kalen JD, Wilan Krisna LA, Hasumi Y, Sugiyama A, Kurahashi R, Nishimoto K, Oyama M, Nagashima Y, Kuroda N, Araki K, Eto M, Yao M, Kamba T, Suda T, Oike Y, Schmidt LS, Linehan WM.

Mol Cancer Res. 2019 Aug;17(8):1613-1626. doi: 10.1158/1541-7786.MCR-18-1235. Epub 2019 May 1.

PMID:
31043488
2.

RBM10-TFE3 renal cell carcinoma characterised by paracentric inversion with consistent closely split signals in break-apart fluorescence in-situ hybridisation: study of 10 cases and a literature review.

Kato I, Furuya M, Baba M, Kameda Y, Yasuda M, Nishimoto K, Oyama M, Yamasaki T, Ogawa O, Niino H, Nakaigawa N, Yano Y, Sakamoto K, Urata Y, Mikami K, Yamasaki S, Tanaka R, Takagi T, Kondo T, Nagashima Y.

Histopathology. 2019 Aug;75(2):254-265. doi: 10.1111/his.13866. Epub 2019 Jun 25.

PMID:
30908700
3.

Hereditary leiomyomatosis and renal cell cancer syndrome in which skin biopsy enabled diagnosis.

Matsuda T, Kambe N, Ly NTM, Ueda-Hayakawa I, Yamazaki F, Ohe C, Yoshida K, Kinoshita H, Furuya M, Okamoto H.

J Dermatol. 2019 Aug;46(8):e285-e287. doi: 10.1111/1346-8138.14855. Epub 2019 Mar 19. No abstract available.

PMID:
30888070
4.

Pathology of Birt-Hogg-Dubé syndrome: A special reference of pulmonary manifestations in a Japanese population with a comprehensive analysis and review.

Furuya M, Nakatani Y.

Pathol Int. 2019 Jan;69(1):1-12. doi: 10.1111/pin.12752. Epub 2019 Jan 11. Review.

PMID:
30632664
5.

A novel partner of TFE3 in the Xp11 translocation renal cell carcinoma: clinicopathological analyses and detection of EWSR1-TFE3 fusion.

Fukuda H, Kato I, Furuya M, Tanaka R, Takagi T, Kondo T, Nagashima Y.

Virchows Arch. 2019 Mar;474(3):389-393. doi: 10.1007/s00428-018-2509-8. Epub 2018 Dec 14.

PMID:
30552521
6.

Hereditary leiomyomatosis and renal cell cancer without cutaneous manifestations in two Japanese siblings.

Noguchi G, Furuya M, Okubo Y, Nagashima Y, Kato I, Matsumoto K, Tanaka R, Hisasue SI, Yao M, Kishida T.

Int J Urol. 2018 Sep;25(9):832-835. doi: 10.1111/iju.13760. Epub 2018 Jul 29.

PMID:
30058172
7.

Medullary carcinoma of the pancreas radiologically followed up as a cystic lesion for 9 years: a case report and review of the literature.

Yago A, Furuya M, Mori R, Yabushita Y, Sawada Y, Kumamoto T, Matsuyama R, Shimizu M, Endo I.

Surg Case Rep. 2018 Jul 24;4(1):80. doi: 10.1186/s40792-018-0487-3.

8.

Parotid Oncocytoma as a Manifestation of Birt-Hogg-Dubé Syndrome.

Yoshida K, Miyagawa M, Kido T, Ide K, Sano Y, Sugawara Y, Takahata H, Monden N, Furuya M, Mochizuki T.

Case Rep Radiol. 2018 Jun 3;2018:6265175. doi: 10.1155/2018/6265175. eCollection 2018.

9.

Histopathological analysis of aggressive renal cell carcinoma harboring a unique germline mutation in fumarate hydratase.

Matsumoto K, Udaka N, Hasumi H, Nakaigawa N, Nagashima Y, Tanaka R, Kato I, Yao M, Furuya M.

Pathol Int. 2018 May 24. doi: 10.1111/pin.12684. [Epub ahead of print]

PMID:
29797630
10.

BHD-associated kidney cancer exhibits unique molecular characteristics and a wide variety of variants in chromatin remodeling genes.

Hasumi H, Furuya M, Tatsuno K, Yamamoto S, Baba M, Hasumi Y, Isono Y, Suzuki K, Jikuya R, Otake S, Muraoka K, Osaka K, Hayashi N, Makiyama K, Miyoshi Y, Kondo K, Nakaigawa N, Kawahara T, Izumi K, Teranishi J, Yumura Y, Uemura H, Nagashima Y, Metwalli AR, Schmidt LS, Aburatani H, Linehan WM, Yao M.

Hum Mol Genet. 2018 May 14. doi: 10.1093/hmg/ddy181. [Epub ahead of print]

11.

Splice-site mutation causing partial retention of intron in the FLCN gene in Birt-Hogg-Dubé syndrome: a case report.

Furuya M, Kobayashi H, Baba M, Ito T, Tanaka R, Nakatani Y.

BMC Med Genomics. 2018 May 2;11(1):42. doi: 10.1186/s12920-018-0359-5.

12.

Giant cell tumours of bone treated with denosumab: histological, immunohistochemical and H3F3A mutation analyses.

Kato I, Furuya M, Matsuo K, Kawabata Y, Tanaka R, Ohashi K.

Histopathology. 2018 May;72(6):914-922. doi: 10.1111/his.13448. Epub 2018 Feb 13.

PMID:
29206281
13.

Review of hereditary leiomyomatosis renal cell carcinoma with focus on clinical and pathobiological aspects of renal tumors.

Kuroda N, Ohe C, Kato I, Furuya M, Baba M, Nagashima Y, Nakatani Y, Murakami I, Zhou M, Michal M, He O, Amin MB.

Pol J Pathol. 2017;68(4):284-290. doi: 10.5114/pjp.2017.73920. Review.

14.

H255Y and K508R missense mutations in tumour suppressor folliculin (FLCN) promote kidney cell proliferation.

Hasumi H, Hasumi Y, Baba M, Nishi H, Furuya M, Vocke CD, Lang M, Irie N, Esumi C, Merino MJ, Kawahara T, Isono Y, Makiyama K, Warner AC, Haines DC, Wei MH, Zbar B, Hagenau H, Feigenbaum L, Kondo K, Nakaigawa N, Yao M, Metwalli AR, Marston Linehan W, Schmidt LS.

Hum Mol Genet. 2017 Jan 15;26(2):354-366. doi: 10.1093/hmg/ddw392.

15.

Establishment and characterization of BHD-F59RSVT, an immortalized cell line derived from a renal cell carcinoma in a patient with Birt-Hogg-Dubé syndrome.

Furuya M, Hasumi H, Baba M, Tanaka R, Iribe Y, Onishi T, Nagashima Y, Nakatani Y, Isono Y, Yao M.

Lab Invest. 2017 Mar;97(3):343-351. doi: 10.1038/labinvest.2016.137. Epub 2016 Dec 19.

16.

Clinical features of Birt-Hogg-Dubé syndrome: A Japanese case with pulmonary cysts, fibrofolliculomas and renal cell carcinoma.

Tanegashima T, Yamaguchi Y, Hamanoue H, Yao M, Furuya M, Aihara M.

J Dermatol. 2017 Dec;44(12):1409-1411. doi: 10.1111/1346-8138.13711. Epub 2016 Dec 10. Review. No abstract available.

PMID:
27943432
17.

Metachronous serous endometrial intraepithelial carcinoma and serous peritoneal carcinoma: analysis of probable independent lesions.

Furuya M, Sato T, Tanaka R, Yamamoto M, Yokota NR, Miyagi E.

Diagn Pathol. 2016 Nov 14;11(1):130.

18.

A Case of Birt-Hogg-Dubé (BHD) Syndrome Harboring a Novel Folliculin (FLCN) Gene Mutation.

Yukawa T, Fukazawa T, Yoshida M, Morita I, Kato K, Monobe Y, Furuya M, Naomoto Y.

Am J Case Rep. 2016 Oct 26;17:788-792.

19.

Genetic, epidemiologic and clinicopathologic studies of Japanese Asian patients with Birt-Hogg-Dubé syndrome.

Furuya M, Yao M, Tanaka R, Nagashima Y, Kuroda N, Hasumi H, Baba M, Matsushima J, Nomura F, Nakatani Y.

Clin Genet. 2016 Nov;90(5):403-412. doi: 10.1111/cge.12807. Epub 2016 Jun 30.

PMID:
27220747
20.

[Pathological Complete Response of Advanced Gastric Cancer after Docetaxel and S-1 Combination Neoadjuvant Chemotherapy-A Case Report].

Arisaka S, Kosaka R, Kunisaki C, Ichikawa Y, Akiyama H, Furuya M, Ohashi K, Endo I.

Gan To Kagaku Ryoho. 2016 Jul;43(7):889-92. Japanese.

PMID:
27431635

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